FDA 510(k) Applications Submitted by TECH-CO, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K921968 | 04/27/1992 | IN VITRO DIAGNOSTIC REAGENT SET, INDIR. PREG. TEST | TECH-CO, INC. |
Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact